EXPLORING NON-INVASIVE DISEASE BIOMARKERS WITH URINARY OMICS ANALYSIS.

Exploring Noninvasive Disease Biomarkers with Urinary Omics Analysis offers a transformative journey into the world of non-invasive diagnostics. This comprehensive volume delves into the molecular foundations of urinary biomarkers, illuminating the intricate signatures that indicate various patholog...

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Bibliographic Details
Corporate Author: ScienceDirect (Online service)
Format: eBook
Language:English
Published: [S.l.] : Academic Press, 2025.
Subjects:
Online Access:Connect to the full text of this electronic book
Table of Contents:
  • Front Cover
  • Exploring Noninvasive Disease Biomarkers with Urinary Omics Analysis
  • Copyright Page
  • Contents
  • List of contributors
  • Foreword
  • Preface
  • 1 Molecular foundations of urinary biomarkers
  • 1.1 Introduction
  • 1.2 Urinary biomarker discovery
  • 1.3 Exploration of urinary biomarkers identified
  • 1.4 Different types of urinary biomarkers
  • 1.4.1 Protein urinary biomarkers
  • 1.4.2 Urinary gene biomarkers
  • 1.4.3 Urinary electrolyte biomarker
  • 1.4.4 Metabolites as urinary biomarkers
  • 1.4.5 Urinary biomarkers of extracellular vesicles
  • 1.5 Role of urine biomarkers in disease diagnosis
  • 1.5.1 Cancer
  • 1.5.1.1 Bladder cancer
  • 1.5.1.2 Prostate cancer
  • 1.5.1.3 Nonurological cancers
  • 1.5.1.4 Cervical cancer
  • 1.5.2 Kidney diseases
  • 1.5.3 Respiratory diseases
  • 1.5.4 Cardiovascular diseases
  • 1.5.5 Neurodegenerative disorders
  • 1.5.6 Diabetes mellitus
  • 1.5.7 Cerebrovascular disease
  • 1.5.8 Trauma
  • 1.5.9 Coagulation disease
  • 1.6 Molecular pathways of urinary biomarker expression
  • 1.7 Analytical techniques for urine biomarkers analysis and validation
  • 1.7.1 Mass spectroscopy
  • 1.7.2 Immunoassay
  • 1.7.3 Capillary electrophoresis
  • 1.7.4 Nuclear magnetic resonance spectroscopy
  • 1.7.5 High-performance liquid chromatography
  • 1.7.6 Polymerase chain reaction and next-generation sequencing
  • 1.8 Point-of-care of urinalysis
  • 1.9 Clinical applications, challenges, and future directions
  • 1.10 Conclusions
  • Abbreviations
  • References
  • 2 Analytical technology: innovations in urinary biomarker discovery
  • 2.1 Introduction
  • 2.2 Origin of urine biomarkers
  • 2.2.1 Sources of urine biomarkers
  • 2.2.2 Types of urine biomarkers
  • 2.3 Analytical technologies
  • 2.3.1 UV-Visible spectroscopy
  • 2.3.1.1 Applications
  • 2.3.1.1.1 Identifying metabolic by-products
  • 2.3.1.1.2 Analysis of proteins.
  • 2.3.1.1.3 Monitoring of substance use
  • 2.3.1.1.4 The identification of abnormal alterations
  • 2.3.1.2 Advantages
  • 2.3.1.3 Disadvantages
  • 2.3.2 Hydrophilic interaction liquid chromatography
  • 2.3.2.1 Applications
  • 2.3.2.1.1 Drug metabolomics and pharmacokinetics
  • 2.3.2.1.2 Environmental and toxicological studies
  • 2.3.2.1.3 Nutritional biomarkers
  • 2.3.2.1.4 Forensic toxicology
  • 2.3.2.2 Advantages
  • 2.3.2.3 Disadvantages
  • 2.3.3 Mass spectrometry
  • 2.3.3.1 Ion source
  • 2.3.3.2 Mass analyzer
  • 2.3.3.3 Detector
  • 2.3.3.4 Applications
  • 2.3.3.4.1 Metabolomics
  • 2.3.3.4.2 Proteomics and peptidomics
  • 2.3.3.4.3 Liquid biopsy
  • 2.3.3.4.4 Pediatric and neonatal biomarkers
  • 2.3.3.4.5 Environmental exposure assessment
  • 2.3.3.5 Advantages
  • 2.3.3.6 Disadvantages
  • 2.4 Proteomics
  • 2.4.1 Goals of proteomics
  • 2.4.2 Methodology for the proteomic analysis of urine biomarkers
  • 2.4.2.1 Liquid chromatography?mass spectrometry
  • 2.4.2.2 Another technique called two-dimensional gel electrophoresis
  • 2.4.2.3 Western blotting
  • 2.4.2.4 Protein microarrays
  • 2.4.2.5 The enzyme-linked immunosorbent assay
  • 2.4.2.6 Stable isotope labeling with amino acids in cell culture
  • 2.4.2.7 Isobaric tags for relative and absolute quantification
  • 2.4.2.8 Surface enhanced laser desorption/ionization (SELDI) a modified form of matrix-assisted laser desorption/ionization
  • 2.4.2.9 Capillary electrophoresis
  • 2.4.2.10 Bioinformatics
  • 2.4.2.11 Urine proteomic analysis workflow involves collecting and preparing samples
  • 2.4.2.12 Applications
  • 2.4.2.12.1 COVID-19 assessing diagnosis and severity
  • 2.4.2.12.2 Emphasizing microbiome health
  • 2.4.2.12.3 Mental health
  • 2.4.2.12.4 Identifying biomarkers
  • 2.4.2.12.5 Urine biomarkers are also being explored to diagnose and manage rare disorders
  • 2.4.2.13 Advantages.
  • 2.4.2.14 Disadvantages
  • 2.5 Metabolomics
  • 2.5.1 Integrated analytical techniques
  • 2.5.1.1 Applications of metabolomics in urine biomarker analysis
  • 2.5.1.1.1 Disease biomarker discovery
  • 2.5.1.1.2 Metabolic disorders
  • 2.5.1.1.3 Environmental and toxicological exposure
  • 2.5.1.1.4 Infectious diseases
  • 2.5.1.2 Advantage
  • 2.5.1.3 Disadvantages
  • 2.6 Multiomics
  • 2.6.1 Applications
  • 2.6.1.1 Cancer
  • 2.6.1.2 Kidney disorder
  • 2.6.1.3 Cardiovascular disease
  • 2.6.1.4 Neurodegenerative disorders
  • 2.6.1.5 Osteoporosis
  • 2.6.2 Advantage
  • 2.6.3 Disadvantages
  • 2.7 Microbiome profiling
  • 2.7.1 Key aspects
  • 2.7.1.1 Microbial species identification
  • 2.7.1.2 Functional analysis
  • 2.7.1.3 Advantages
  • 2.7.1.4 Disadvantages
  • 2.8 Enzyme-linked immunosorbent assay
  • 2.8.1 Types of enzyme-linked immunosorbent assay
  • 2.8.1.1 General methodology
  • 2.8.1.2 Applications
  • 2.8.1.3 Advantages
  • 2.8.1.4 Disadvantages
  • 2.9 Multiplex protein detection immunoassay
  • 2.9.1 Applications
  • 2.9.2 Advantages
  • 2.9.3 Disadvantages
  • 2.10 Single antibody array chips
  • 2.10.1 Working
  • 2.10.1.1 Applications
  • 2.10.1.2 Advantages
  • 2.10.1.3 Disadvantages
  • 2.11 Advanced statistical methodologies
  • 2.11.1 Statistical techniques and their applications
  • 2.11.1.1 Multivariate analysis
  • 2.11.1.2 Machine learning algorithms
  • 2.11.1.3 Bayesian inference
  • 2.11.2 Software tools
  • 2.11.3 Visualization tools
  • 2.12 Conclusion
  • AI disclosure
  • References
  • 3 Infectious disease diagnostics: insights from urinary omics
  • 3.1 Introduction
  • 3.2 The emergence of urinary omics as an infectious disease diagnostic tool
  • 3.3 Scope and impact of urinary omics on infectious disease detection
  • 3.4 Technological advancements in urinary omics
  • 3.4.1 High-throughput sequencing and metabolomic profiling techniques.
  • 3.4.2 Innovations in bioinformatics for data analysis and interpretation
  • 3.4.3 Integration of omics data: a multidimensional approach
  • 3.5 Pathogen detection and biomarker identification
  • 3.5.1 Strategies for pathogen-specific biomarker discovery
  • 3.5.2 Characterization of host response signatures to infection
  • 3.5.3 Differential biomarker expression and pathogenicity
  • 3.6 Clinical case studies: urinary omics in action
  • 3.6.1 Case studies
  • 3.6.1.1 Recurrent urinary tract infections studied using urinary omics approaches
  • 3.6.1.1.1 Genomic insights into recurrent urinary tract infections
  • 3.6.1.1.2 Proteomic analysis of recurrent urinary tract infections
  • 3.6.1.1.3 Metabolomic profiling in recurrent urinary tract infections
  • 3.6.1.1.4 Microbiomic contributions to recurrent urinary tract infections
  • 3.6.1.1.5 Integrative omics approaches to recurrent urinary tract infections
  • 3.6.1.2 Tuberculosis studied using urinary omics approaches
  • 3.6.1.2.1 Genomic insights into tuberculosis using urinary samples
  • 3.6.1.2.2 Proteomic analysis of urine in tuberculosis
  • 3.6.1.2.3 Metabolomic profiling in tuberculosis
  • 3.6.1.2.4 Microbiomic contributions to tuberculosis diagnosis and management
  • 3.6.1.2.5 Integrative omics approaches
  • 3.6.1.3 COVID-19 studied using urinary omics approaches
  • 3.6.1.3.1 Genomic insights into COVID-19 using urinary samples
  • 3.6.1.3.2 Proteomic analysis of urine in COVID-19
  • 3.6.1.3.3 Metabolomic profiling in COVID-19
  • 3.6.1.3.4 Microbiomic contributions to COVID-19 diagnosis and management
  • 3.6.1.3.5 Integrative omics approaches
  • 3.6.2 Comparative analysis with traditional diagnostic methods
  • 3.6.3 Urinary omics in emerging and reemerging infectious diseases
  • 3.7 Challenges and considerations in urinary omics diagnostics
  • 3.7.1 Sample collection and standardization issue.
  • 3.7.2 Sensitivity, specificity, and predictive value of omics-based tests
  • 3.7.2.1 Sensitivity and specificity challenges
  • 3.7.2.2 Standardization and biomarker degradation
  • 3.7.2.3 Bioinformatics and predictive value
  • 3.7.3 Ethical, legal, and social implications of omics data
  • 3.7.3.1 Ethical considerations
  • 3.7.3.2 Legal implications
  • 3.7.3.3 Social implications
  • 3.8 Future directions and potential of urinary omics
  • 3.8.1 Next-generation technologies and their prospective impact
  • 3.8.2 Bridging the gap between research and clinical practice
  • 3.8.3 Global health perspectives and accessibility of omics diagnostics
  • 3.9 Conclusion
  • AI disclosure
  • References
  • 4 Standardizing sample preparation: ensuring integrity in urinary omics
  • 4.1 Introduction
  • 4.2 Sample preparation and preprocessing
  • 4.2.1 Processing of urine samples
  • 4.2.2 Optimizing omics research practices
  • 4.2.3 Heel stick sample
  • 4.2.4 Impact of external factors on sample integrity
  • 4.2.4.1 Temperature
  • 4.2.4.2 pH
  • 4.2.4.3 Time
  • 4.2.4.4 Other parameters
  • 4.2.5 Strategies for minimizing preanalytical variability
  • 4.3 Sample processing
  • 4.3.1 Metabolic quenching in urinary omics
  • 4.3.2 Centrifugation and filtration in Extracellular Vesicles (EV) isolation
  • 4.3.3 Aliquoting and storage
  • 4.3.4 Thawing of samples
  • 4.3.5 Quality control measures
  • 4.4 Analytical techniques for diagnosing urinary problems
  • 4.4.1 Overview of urinary omics analytical techniques
  • 4.4.2 Pros and cons
  • 4.4.2.1 Limitations of surface-enhanced laser desorption/ionization-TOF mass spectrometry
  • 4.4.2.2 Limitations of capillary electrophoresis-mass spectrometry in urinary proteomics
  • 4.4.3 Considerations for sample preparation
  • 4.5 Data analysis
  • 4.5.1 Overview of data analysis techniques
  • 4.5.2 Quality control measures.